Ethyl 3-hydroxy-3-methylbutyrate

Details

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Internal ID c8ad3d6c-70e9-4eb1-b810-c11dfac51cfc
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl 3-hydroxy-3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H14O3/c1-4-10-6(8)5-7(2,3)9/h9H,4-5H2,1-3H3
InChI Key HKEDUIGHSRRIKD-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14O3
Molecular Weight 146.18 g/mol
Exact Mass 146.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.71
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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18267-36-2
Ethyl 3-hydroxy-3-methylbutyrate
EINECS 242-147-5
DTXSID70171317
RefChem:594975
DTXCID9093808
242-147-5
Butanoic acid, 3-hydroxy-3-methyl-, ethyl ester
MFCD16749012
Ethyl3-hydroxy-3-methylbutanoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl 3-hydroxy-3-methylbutyrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.8843 88.43%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8269 82.69%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9547 95.47%
OATP1B3 inhibitior + 0.9568 95.68%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8899 88.99%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9909 99.09%
CYP3A4 substrate - 0.6072 60.72%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.8698 86.98%
CYP3A4 inhibition - 0.9161 91.61%
CYP2C9 inhibition - 0.8842 88.42%
CYP2C19 inhibition - 0.8496 84.96%
CYP2D6 inhibition - 0.9367 93.67%
CYP1A2 inhibition - 0.8665 86.65%
CYP2C8 inhibition - 0.9636 96.36%
CYP inhibitory promiscuity - 0.9177 91.77%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.4983 49.83%
Eye corrosion + 0.5798 57.98%
Eye irritation + 0.9960 99.60%
Skin irritation - 0.7498 74.98%
Skin corrosion - 0.9282 92.82%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7132 71.32%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5599 55.99%
skin sensitisation + 0.5129 51.29%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5784 57.84%
Acute Oral Toxicity (c) III 0.8658 86.58%
Estrogen receptor binding - 0.9547 95.47%
Androgen receptor binding - 0.9712 97.12%
Thyroid receptor binding - 0.8598 85.98%
Glucocorticoid receptor binding - 0.9295 92.95%
Aromatase binding - 0.8820 88.20%
PPAR gamma - 0.9234 92.34%
Honey bee toxicity - 0.9459 94.59%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.6775 67.75%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.37% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.15% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.38% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 84.05% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.61% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 80.04% 89.63%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Hippophae rhamnoides

Cross-Links

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PubChem 87537
NPASS NPC230881
LOTUS LTS0052095
wikiData Q83041392